Laser Optical Sensor, a Label-Free On-Plate Salmonella enterica Colony Detection Tool

ABSTRACT We investigated the application capabilities of a laser optical sensor, BARDOT (bacterial rapid detection using optical scatter technology) to generate differentiating scatter patterns for the 20 most frequently reported serovars of Salmonella enterica. Initially, the study tested the classification ability of BARDOT by using six Salmonella serovars grown on brain heart infusion, brilliant green, xylose lysine deoxycholate, and xylose lysine tergitol 4 (XLT4) agar plates. Highly accurate discrimination (95.9%) was obtained by using scatter signatures collected from colonies grown on XLT4. Further verification used a total of 36 serovars (the top 20 plus 16) comprising 123 strains with classification precision levels of 88 to 100%. The similarities between the optical phenotypes of strains analyzed by BARDOT were in general agreement with the genotypes analyzed by pulsed-field gel electrophoresis (PFGE). BARDOT was evaluated for the real-time detection and identification of Salmonella colonies grown from inoculated (1.2 × 102 CFU/30 g) peanut butter, chicken breast, and spinach or from naturally contaminated meat. After a sequential enrichment in buffered peptone water and modified Rappaport Vassiliadis broth for 4 h each, followed by growth on XLT4 (~16 h), BARDOT detected S. Typhimurium with 84% accuracy in 24 h, returning results comparable to those of the USDA Food Safety and Inspection Service method, which requires ~72 h. BARDOT also detected Salmonella (90 to 100% accuracy) in the presence of background microbiota from naturally contaminated meat, verified by 16S rRNA sequencing and PFGE. Prolonged residence (28 days) of Salmonella in peanut butter did not affect the bacterial ability to form colonies with consistent optical phenotypes. This study shows BARDOT’s potential for nondestructive and high-throughput detection of Salmonella in food samples. IMPORTANCE High-throughput screening of food products for pathogens would have a significant impact on the reduction of food-borne hazards. A laser optical sensor was developed to screen pathogen colonies on an agar plate instantly without damaging the colonies; this method aids in early pathogen detection by the classical microbiological culture-based method. Here we demonstrate that this sensor was able to detect the 36 Salmonella serovars tested, including the top 20 serovars, and to identify isolates of the top 8 Salmonella serovars. Furthermore, it can detect Salmonella in food samples in the presence of background microbiota in 24 h, whereas the standard USDA Food Safety and Inspection Service method requires about 72 h. High-throughput screening of food products for pathogens would have a significant impact on the reduction of food-borne hazards. A laser optical sensor was developed to screen pathogen colonies on an agar plate instantly without damaging the colonies; this method aids in early pathogen detection by the classical microbiological culture-based method. Here we demonstrate that this sensor was able to detect the 36 Salmonella serovars tested, including the top 20 serovars, and to identify isolates of the top 8 Salmonella serovars. Furthermore, it can detect Salmonella in food samples in the presence of background microbiota in 24 h, whereas the standard USDA Food Safety and Inspection Service method requires about 72 h.

[1]  Mieke Uyttendaele,et al.  Alternative microbial methods: An overview and selection criteria. , 2010, Food microbiology.

[2]  E Ben-Jacob,et al.  Cooperative organization of bacterial colonies: from genotype to morphotype. , 1998, Annual review of microbiology.

[3]  Euiwon Bae,et al.  On the sensitivity of forward scattering patterns from bacterial colonies to media composition , 2011, Journal of biophotonics.

[4]  J. Paul Robinson,et al.  Biophysical modeling of forward scattering from bacterial colonies using scalar diffraction theory. , 2007, Applied optics.

[5]  J. Folster,et al.  Outbreak of Salmonella Heidelberg Infections Linked to a Single Poultry Producer — 13 States, 2012–2013 , 2013, MMWR. Morbidity and mortality weekly report.

[6]  B. Kuehn Salmonella cases traced to egg producers: findings trigger recall of more than 500 million eggs. , 2010, JAMA.

[7]  G. Olsen,et al.  Comparative genomics of closely related salmonellae. , 2002, Trends in microbiology.

[8]  J. Paul Robinson,et al.  Discovering the unknown: Detection of emerging pathogens using a label‐free light‐scattering system , 2010, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

[9]  C. Hinshelwood,et al.  Factors affecting the growth of bacterial colonies on agar plates , 1968, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[10]  Shu-I Tu,et al.  Evanescent Wave Fiber Optic Biosensor for Salmonella Detection in Food , 2009, Sensors.

[11]  M. Gordon Invasive nontyphoidal Salmonella disease: epidemiology, pathogenesis and diagnosis , 2011, Current opinion in infectious diseases.

[12]  P. Fields,et al.  Multiplex, Bead-Based Suspension Array for Molecular Determination of Common Salmonella Serogroups , 2007, Journal of Clinical Microbiology.

[13]  I. Wachsmuth,et al.  Powdered infant formula as a source of Salmonella infection in infants. , 2008, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[14]  P. Fratamico,et al.  Strengths and Shortcomings of Advanced Detection Technologies , 2011 .

[15]  Chukuka S Enwemeka,et al.  Blue 470-nm light kills methicillin-resistant Staphylococcus aureus (MRSA) in vitro. , 2009, Photomedicine and laser surgery.

[16]  E. Alocilja,et al.  A multiplex nanoparticle-based bio-barcoded DNA sensor for the simultaneous detection of multiple pathogens. , 2010, Biosensors & bioelectronics.

[17]  H. Shu,et al.  Image description with generalized pseudo-Zernike moments. , 2007, Journal of the Optical Society of America. A, Optics, image science, and vision.

[18]  Fred C Tenover,et al.  Rapid detection and identification of bacterial pathogens using novel molecular technologies: infection control and beyond. , 2007, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[19]  A. Singh,et al.  Evaluation of a facile method of template DNA preparation for PCR-based detection and typing of lactic acid bacteria. , 2009, Food microbiology.

[20]  Scott Nowicki,et al.  Multistate outbreak of Salmonella infections associated with peanut butter and peanut butter-containing products--United States, 2008-2009. , 2009, MMWR. Morbidity and mortality weekly report.

[21]  D. Yeh,et al.  Designing of polymerase chain reaction primers for the detection of Salmonella enteritidis in foods and faecal samples , 2002, Letters in applied microbiology.

[22]  A. Lynne,et al.  Food animal-associated Salmonella challenges: pathogenicity and antimicrobial resistance. , 2008, Journal of animal science.

[23]  R. Dieckmann,et al.  Rapid Screening of Epidemiologically Important Salmonella enterica subsp. enterica Serovars by Whole-Cell Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry , 2011, Applied and Environmental Microbiology.

[24]  Pierre Wattiau,et al.  Methodologies for Salmonella enterica subsp. enterica Subtyping: Gold Standards and Alternatives , 2011, Applied and Environmental Microbiology.

[25]  P. Fields,et al.  Molecular Determination of H Antigens of Salmonella by Use of a Microsphere-Based Liquid Array , 2010, Journal of Clinical Microbiology.

[26]  S. Sela,et al.  Effect of Desiccation on Tolerance of Salmonella enterica to Multiple Stresses , 2011, Applied and Environmental Microbiology.

[27]  M. Wilson,et al.  Sensitization of periodontopathogenic bacteria to killing by light from a low-power laser. , 1993, Oral microbiology and immunology.

[28]  J Hoorfar Rapid detection, characterization, and enumeration of foodborne pathogens , 2011, APMIS. Supplementum.

[29]  A. Bhunia,et al.  Highly specific fiber optic immunosensor coupled with immunomagnetic separation for detection of low levels of Listeria monocytogenes and L. ivanovii , 2012, BMC Microbiology.

[30]  Willem Haasnoot,et al.  Multiplex bioanalytical methods for food and environmental monitoring , 2011, TrAC Trends in Analytical Chemistry.

[31]  D. G. Black,et al.  Sources and risk factors for contamination, survival, persistence, and heat resistance of Salmonella in low-moisture foods. , 2010, Journal of food protection.

[32]  Improved detection of nontyphoid and typhoid Salmonellae with balanced agar formulations. , 2000, Journal of food protection.

[33]  S. Palumbo,et al.  Growth measurements on surface colonies of bacteria. , 1971, Journal of general microbiology.

[34]  S. Puthucheary,et al.  Simple and rapid detection of Salmonella strains by direct PCR amplification of the hilA gene. , 2003, Journal of medical microbiology.

[35]  J. Frye,et al.  Sensitive and rapid molecular detection assays for Salmonella enterica serovars Typhimurium and Heidelberg. , 2009, Journal of food protection.

[36]  A. Bhunia,et al.  Human heat‐shock protein 60 receptor‐coated paramagnetic beads show improved capture of Listeria monocytogenes in the presence of other Listeria in food , 2011, Journal of applied microbiology.

[37]  J. Paul Robinson,et al.  Analysis of time-resolved scattering from macroscale bacterial colonies. , 2008, Journal of biomedical optics.

[38]  M. Widdowson,et al.  Foodborne Illness Acquired in the United States—Major Pathogens , 2011, Emerging infectious diseases.

[39]  J. Paul Robinson,et al.  Feature extraction from light-scatter patterns of Listeria colonies for identification and classification. , 2006, Journal of biomedical optics.

[40]  Yating Chai,et al.  Rapid and sensitive detection of Salmonella Typhimurium on eggshells by using wireless biosensors. , 2012, Journal of food protection.

[41]  M. Bissell Multiplex, Bead-Based Suspension Array for Molecular Determination of Common Salmonella Serogroups , 2009 .

[42]  M. Bülte,et al.  A comparison of standard cultural methods for the detection of foodborne Salmonella species including three new chromogenic plating media. , 2008, International journal of food microbiology.

[43]  J. Prescott,et al.  Development of a Novel Protein Microarray Method for Serotyping Salmonella enterica Strains , 2005, Journal of Clinical Microbiology.

[44]  A. Bhunia,et al.  Salmonella in pork, beef, poultry, and egg. , 2011 .

[45]  A. Bhunia RAPID PATHOGEN SCREENING TOOLS FOR FOOD SAFETY , 2011 .

[46]  Michael C. McAlpine,et al.  Electrical detection of pathogenic bacteria via immobilized antimicrobial peptides , 2010, Proceedings of the National Academy of Sciences.

[47]  M. Moore,et al.  Real‐time PCR method for Salmonella spp. targeting the stn gene , 2007, Journal of applied microbiology.

[48]  J. Paul Robinson,et al.  Light‐scattering sensor for real‐time identification of Vibrio parahaemolyticus, Vibrio vulnificus and Vibrio cholerae colonies on solid agar plate , 2012, Microbial biotechnology.

[49]  E. Mallinson,et al.  Xylose-lysine-tergitol 4: an improved selective agar medium for the isolation of Salmonella. , 1991, Poultry science.

[50]  B. Swaminathan,et al.  Standardization of pulsed-field gel electrophoresis protocols for the subtyping of Escherichia coli O157:H7, Salmonella, and Shigella for PulseNet. , 2006, Foodborne pathogens and disease.

[51]  J. Paul Robinson,et al.  Label-free detection of multiple bacterial pathogens using light-scattering sensor. , 2009, Biosensors & bioelectronics.

[52]  Arun K Bhunia,et al.  Biosensors and bio-based methods for the separation and detection of foodborne pathogens. , 2008, Advances in food and nutrition research.

[53]  J. Paul Robinson,et al.  Optical forward-scattering for detection of Listeria monocytogenes and other Listeria species. , 2007, Biosensors & bioelectronics.